Newsletter | April 17, 2026

04.17.26 -- How Outsourcing Meets Precision: A Formula For CDMO Interactions

SPONSOR

Join Outsourced Pharmaceutical Live’s Jeff Buguliskis and panelists on April 22nd at 11 AM Eastern for One Program, Many CDMOs: Managing Multi-Partner Strategies. Registration for this virtual event is free thanks to sponsor Thermo Fisher.

INDUSTRY INSIGHTS

Clinical And Formulation Strategies For Targeted Peptide Drug Development

Novel technologies and therapies are helping drug developers to overcome challenges associated with the development of injectable and oral peptide formulations.

Mitigating Powder Flow And Static Issues

See how incorporating small amounts of mesoporous silica during micronization can significantly enhance powder flow, thereby making subsequent blending and formulation more consistent.

A Powerful Non-Destructive Tool For Tablet Characterization

Assimilate how X-ray micro-CT provides vital, non-destructive analysis of a tablet’s internal 3D physical structure. This structural insight is essential for troubleshooting defects and confirming performance.

FEATURED EDITORIAL

How Outsourcing Meets Precision: A Formula For CDMO Interactions

Seema Singh of Daiichi Sankyo represents today’s global regulatory leadership in the biopharmaceutical sector. She reflects what the highest expectations should be for all CDMOs, whether your organization is an exacting Japan Pharma, or a start-up biotech in the U.S. Here are her key actions for creating an optimal outsourcing relationship.

New ISPE Framework Targets Uncertainty In Pharma's AI Deployment

International Society for Pharmaceutical Engineering members developed the guide to offer a risk-based framework for evaluating, implementing, and maintaining AI systems.

INDUSTRY INSIGHTS CONTINUED

GLP Compliance In A Modern Lab

GLP compliance isn’t binary. Real defensibility depends on rigorous QA, validated electronic systems, and operational maturity — not just a label.

Reshaping Drug Development With 3D Screen Printing

Steven Facer and Laxxon Medical COO Klaus Kühne describe the capabilities of 3D screen printing for pharmaceutical production. Explore prototyping, IP protection, release profile possibilities, and more.

SPONSOR

Outsourced Pharma Capabilities Update

This online event series connects biopharma companies with CDMOs to explore capabilities across biologics production, HPAPI manufacturing, and drug–device combination development. Through concise presentations, CDMOs showcase expertise in development, scale-up, containment, and GMP manufacturing. Attendees gain insights into technologies, regulatory expectations, and partnership models, while engaging directly with providers to evaluate outsourcing options and identify the best-fit partners for advancing and commercializing complex therapies. Click to learn more.

SOLUTIONS

Integrated Quality, Regulatory, And Safety Services

A single-vendor model for quality and safety services provides consistent project management and cost-effective scalability. Hear how integrated solutions support market entry and growth.

In-Silico Modeling Services

In silico modeling technologies are transforming drug development and manufacturing by enhancing efficiency, accuracy, to allow innovations.

Solid Form Services

We have defined work flows to assess and select solid forms in a cost and time efficient manner that meets the needs of each individual program.

OUTSOURCED PHARMA CAPABILITIES UPDATE

Find Your New CDMO At Outsourced Pharma Capabilities Update

CDMOs in biologics, cell and gene, and small molecule share their capabilities and available capabilities. See for yourself why this virtual event has become a wildly popular resource to identify options for your development and manufacturing needs.

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